scholarly journals From stem cell to erythroblast: Regulation of red cell production at multiple levels by multiple hormones

IUBMB Life ◽  
2010 ◽  
Vol 62 (7) ◽  
pp. 492-496 ◽  
Author(s):  
Harvey Lodish ◽  
Johan Flygare ◽  
Song Chou
Blood ◽  
2011 ◽  
Vol 118 (21) ◽  
pp. SCI-1-SCI-1 ◽  
Author(s):  
Harvey F. Lodish

Abstract SCI-1 Hematopoietic stem cells (HSC) undergo self-renewal and also generate all types of blood cells, including red cells, myeloid cells, and all immune system cells. Formation of red cells from HSC involves multiple cellular stages, including early erythroid-specific progenitors (burst-forming unit-erythroid [BFU-E]) that respond to several growth factors and an erythropoietin (Epo)-responsive progenitor, and the colony-forming unit-erythroid (CFU-E) that in 3 days generates ∼30 reticulocytes. In adult animals most CFU-E cells undergo apoptosis. A short-term need for red cells is met by increased Epo production by the kidney, which rescues increasing numbers of CFU-Es from apoptosis and increases red cell production over a few days. Chronic stress, such as in certain types of anemias and inflammatory diseases, leads to a marked increase in numbers of HSC and many types of progenitor cells. I will focus most of my talk on stress-triggered BFU-E proliferation and formation of CFU-Es, since our very recent work showed how glucocorticoids – an important class of stress hormones – as well as HIF-1α stimulate red cell production. Acting synergistically these allow ∼300 times more CFU-Es and erythroblasts to be formed from each BFU-E. More specifically, these molecules stimulate limited self-renewal of BFU-Es during cell division, thus maintaining progenitor immaturity and allowing over time increased numbers of CFU-E cells and thus mature red cells to be formed. This explains why certain corticosteroids are useful in treating some non-Epo responsive anemias, and I will present a molecular dissection of glucocorticoid and HIF-1α action on BFU-E progenitors that has led to the identification of genes critical for self-renewal and that suggest other possible avenues for treatment of chronic anemias. Disclosures: No relevant conflicts of interest to declare.


Blood ◽  
2011 ◽  
Vol 118 (24) ◽  
pp. 6258-6268 ◽  
Author(s):  
Shilpa M. Hattangadi ◽  
Piu Wong ◽  
Lingbo Zhang ◽  
Johan Flygare ◽  
Harvey F. Lodish

Abstract This article reviews the regulation of production of RBCs at several levels. We focus on the regulated expansion of burst-forming unit-erythroid erythroid progenitors by glucocorticoids and other factors that occur during chronic anemia, inflammation, and other conditions of stress. We also highlight the rapid production of RBCs by the coordinated regulation of terminal proliferation and differentiation of committed erythroid colony-forming unit-erythroid progenitors by external signals, such as erythropoietin and adhesion to a fibronectin matrix. We discuss the complex intracellular networks of coordinated gene regulation by transcription factors, chromatin modifiers, and miRNAs that regulate the different stages of erythropoiesis.


1968 ◽  
Vol 122 (3) ◽  
pp. 230-235 ◽  
Author(s):  
A. J. Erslev
Keyword(s):  
Red Cell ◽  

2021 ◽  
Vol 33 ◽  
pp. 369-379
Author(s):  
László Monostori ◽  
Balázs Cs. Csáji ◽  
Péter Egri ◽  
Krisztián B. Kis ◽  
József Váncza ◽  
...  
Keyword(s):  

JAMA ◽  
1963 ◽  
Vol 184 (5) ◽  
pp. 432
Author(s):  
Leon O. Jacobson
Keyword(s):  
Red Cell ◽  

1952 ◽  
Vol 7 (3) ◽  
pp. 129-143 ◽  
Author(s):  
Rex L. Huff ◽  
Cornelius A. Tobias ◽  
John H. Lawrence
Keyword(s):  
Red Cell ◽  

2014 ◽  
pp. 1-1
Author(s):  
Ramadas Nayak ◽  
Sharada Rai
Keyword(s):  
Red Cell ◽  

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